RA People, Powering Up Your Regulatory Team
The new Medical Device Regulation (MDR) brings a period of major change, uncertainty, and new opportunities in the market of medical technology and diagnostics. The expectation is that there will be significant shortages of trained specialists with the right knowledge and experience.
RA People recruits and places candidates, and trains them to be Regulatory Affairs Specialists.
RA Specialists are people who ensure that medical devices meet the applicable standards and laws. RA Specialists know how to translate legal and regulatory requirements for medical devices into requirements for the organisation and the products.